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60. Hajipour AR, Abolfathi P (2017) Novel triazole-modified chitosan@nickel nanoparticles:
efficient and recoverable catalysts for Suzuki reaction. New J Chem 41(6):2386–2391. https://
doi.org/10.1039/C6NJ03789E
61. Hajipour AR, Rezaei F, Khorsandi Z (2017) Pd/Cu-free Heck and Sonogashira cross-coupling
reaction by Co nanoparticles immobilized on magnetic chitosan as reusable catalyst. Green
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62. Handa S, Slack ED, Lipshutz BH (2015) Nanonickel-catalyzed Suzuki–Miyaura crosscouplings in water. Angew Chem Int 54(41):11994–11998. https://doi.org/10.1002/anie.
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63. Heiz U, Landman U (eds) (2007) Nanocatalysis. Springer, Berlin
64. Heravi MM, Zadsirjan V, Hajiabbasi P, Hamidi H (2019) Advances in Kumada–Tamao–Corriu
cross-coupling reaction: an update. Monatsh Chem 150(4):535–591. https://doi.org/10.1007/
s00706-019-2364-6
65. Irrgang T, Kempe R (2019) 3d-metal catalyzed N- and C-alkylation reactions via borrowing
hydrogen or hydrogen autotransfer. Chem Rev 119(4):2524–2549. https://doi.org/10.1021/
acs.chemrev.8b00306
66. Joule JA, Mills K (2013) Heterocyclic chemistry at a glance, 2 nd Edition. John Wiley & sons,
Sussex
67. Kataria M, Pramanik S, Kaur N, Kumar M, Bhalla V (2016) Ferromagnetic α-Fe 2 O 3 NPs: a
potential catalyst in Sonogashira-Hagihara cross coupling and hetero-Diels–Alder reactions.
Green Chem 18(6):1495–1505. https://doi.org/10.1039/C5GC02337H
68. Kaushik M, Moores A (2017) New trends in sustainable nanocatalysis: emerging use of earth
abundant metals. Curr Opin Green Sustain Chem 7:39–45. https://doi.org/10.1016/j.cogsc.
2017.07.002
69. Kerton F, Marriott R (2013) Alternative solvents for green chemistry, Edition 2. RSC
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70. Kharasch MS, Fields EK (1941) Factors determining the course and mechanisms of Grignard
reactions. IV. The effect of metallic halides on the reaction of aryl grignard reagents and
organic halides 1. J Am Chem Soc 63(9):2316–2320. https://doi.org/10.1021/ja01854a006
71. Khurana JM, Vij K (2010) Nickel nanoparticles catalyzed Knoevenagel condensation of aromatic aldehydes with barbituric acids and 2-thiobarbituric acids. Catal Lett 138(1):104–110.
https://doi.org/10.1007/s10562-010-0376-2
72. Khurana JM, Vij K (2011) Nickel nanoparticles catalyzed chemoselective Knoevenagel condensation of Meldrum’s acid and tandem enol lactonizations via cascade cyclization sequence.
Tetrahedron Lett 52(28):3666–3669. https://doi.org/10.1016/j.tetlet.2011.05.032
73. Khurana JM, Yadav S (2012) Highly monodispersed PEG-stabilized Ni nanoparticles:
proficient catalyst for the synthesis of biologically important spiropyrans. Aust J Chem
65(3):314–319. https://doi.org/10.1071/CH11444
74. Kidwai M, Mishra NK, Bhardwaj S, Jahan A, Kumar A, Mozumdar S (2010) Cu nanoparticles in PEG: a new recyclable catalytic system for N-arylation of amines with aryl halides.
ChemCatChem 2(10):1312–1317. https://doi.org/10.1002/cctc.201000062
75. Klajn R (2014) Spiropyran-based dynamic materials. Chem Soc Rev 43(1):148–184. https://
doi.org/10.1039/C3CS60181A
76. Kotovshchikov YN, Latyshev GV, Lukashev NV, Beletskaya IP (2015) Alkynylation of
steroids via Pd-free Sonogashira coupling. Org Biomol Chem 13(19):5542–5555. https://
doi.org/10.1039/C5OB00559K
77. Kunz K, Scholz U, Ganzer D (2003) Renaissance of Ullmann and Goldberg reactions—
progress in copper catalyzed C-N-C-O- and C-S-coupling. Synlett 2003(15):2428–2439.
https://doi.org/10.1055/s-2003-42473
78. LaGrow AP, Ingham B, Cheong S, Williams GVM, Dotzler C, Toney MF, Tilley RD (2012)
Synthesis, alignment, and magnetic properties of monodisperse nickel nanocubes. J Am Chem
Soc 134(2):855–858. https://doi.org/10.1021/ja210209r
M. Camats et al.
59. Haji M (2016) Multicomponent reactions: a simple and efficient route to heterocyclic
phosphonates. Beilstein J Org Chem 12:1269–1301. https://doi.org/10.3762/bjoc.12.121
60. Hajipour AR, Abolfathi P (2017) Novel triazole-modified chitosan@nickel nanoparticles:
efficient and recoverable catalysts for Suzuki reaction. New J Chem 41(6):2386–2391. https://
doi.org/10.1039/C6NJ03789E
61. Hajipour AR, Rezaei F, Khorsandi Z (2017) Pd/Cu-free Heck and Sonogashira cross-coupling
reaction by Co nanoparticles immobilized on magnetic chitosan as reusable catalyst. Green
Chem 19(5):1353–1361. https://doi.org/10.1039/C6GC03377F
62. Handa S, Slack ED, Lipshutz BH (2015) Nanonickel-catalyzed Suzuki–Miyaura crosscouplings in water. Angew Chem Int 54(41):11994–11998. https://doi.org/10.1002/anie.
201505136
63. Heiz U, Landman U (eds) (2007) Nanocatalysis. Springer, Berlin
64. Heravi MM, Zadsirjan V, Hajiabbasi P, Hamidi H (2019) Advances in Kumada–Tamao–Corriu
cross-coupling reaction: an update. Monatsh Chem 150(4):535–591. https://doi.org/10.1007/
s00706-019-2364-6
65. Irrgang T, Kempe R (2019) 3d-metal catalyzed N- and C-alkylation reactions via borrowing
hydrogen or hydrogen autotransfer. Chem Rev 119(4):2524–2549. https://doi.org/10.1021/
acs.chemrev.8b00306
66. Joule JA, Mills K (2013) Heterocyclic chemistry at a glance, 2 nd Edition. John Wiley & sons,
Sussex
67. Kataria M, Pramanik S, Kaur N, Kumar M, Bhalla V (2016) Ferromagnetic α-Fe 2 O 3 NPs: a
potential catalyst in Sonogashira-Hagihara cross coupling and hetero-Diels–Alder reactions.
Green Chem 18(6):1495–1505. https://doi.org/10.1039/C5GC02337H
68. Kaushik M, Moores A (2017) New trends in sustainable nanocatalysis: emerging use of earth
abundant metals. Curr Opin Green Sustain Chem 7:39–45. https://doi.org/10.1016/j.cogsc.
2017.07.002
69. Kerton F, Marriott R (2013) Alternative solvents for green chemistry, Edition 2. RSC
Publishing
70. Kharasch MS, Fields EK (1941) Factors determining the course and mechanisms of Grignard
reactions. IV. The effect of metallic halides on the reaction of aryl grignard reagents and
organic halides 1. J Am Chem Soc 63(9):2316–2320. https://doi.org/10.1021/ja01854a006
71. Khurana JM, Vij K (2010) Nickel nanoparticles catalyzed Knoevenagel condensation of aromatic aldehydes with barbituric acids and 2-thiobarbituric acids. Catal Lett 138(1):104–110.
https://doi.org/10.1007/s10562-010-0376-2
72. Khurana JM, Vij K (2011) Nickel nanoparticles catalyzed chemoselective Knoevenagel condensation of Meldrum’s acid and tandem enol lactonizations via cascade cyclization sequence.
Tetrahedron Lett 52(28):3666–3669. https://doi.org/10.1016/j.tetlet.2011.05.032
73. Khurana JM, Yadav S (2012) Highly monodispersed PEG-stabilized Ni nanoparticles:
proficient catalyst for the synthesis of biologically important spiropyrans. Aust J Chem
65(3):314–319. https://doi.org/10.1071/CH11444
74. Kidwai M, Mishra NK, Bhardwaj S, Jahan A, Kumar A, Mozumdar S (2010) Cu nanoparticles in PEG: a new recyclable catalytic system for N-arylation of amines with aryl halides.
ChemCatChem 2(10):1312–1317. https://doi.org/10.1002/cctc.201000062
75. Klajn R (2014) Spiropyran-based dynamic materials. Chem Soc Rev 43(1):148–184. https://
doi.org/10.1039/C3CS60181A
76. Kotovshchikov YN, Latyshev GV, Lukashev NV, Beletskaya IP (2015) Alkynylation of
steroids via Pd-free Sonogashira coupling. Org Biomol Chem 13(19):5542–5555. https://
doi.org/10.1039/C5OB00559K
77. Kunz K, Scholz U, Ganzer D (2003) Renaissance of Ullmann and Goldberg reactions—
progress in copper catalyzed C-N-C-O- and C-S-coupling. Synlett 2003(15):2428–2439.
https://doi.org/10.1055/s-2003-42473
78. LaGrow AP, Ingham B, Cheong S, Williams GVM, Dotzler C, Toney MF, Tilley RD (2012)
Synthesis, alignment, and magnetic properties of monodisperse nickel nanocubes. J Am Chem
Soc 134(2):855–858. https://doi.org/10.1021/ja210209r